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Assessment of half-mask elastomeric respirator and powered airpurifying respirator reprocessing for an influenza pandemic

Identifieur interne : 000854 ( Pmc/Corpus ); précédent : 000853; suivant : 000855

Assessment of half-mask elastomeric respirator and powered airpurifying respirator reprocessing for an influenza pandemic

Auteurs : Caryn Lawrence ; Delbert A. Harnish ; Megan Sandoval-Powers ; Devin Mills ; Michael Bergman ; Brian K. Heimbuch

Source :

RBID : PMC:6193495

Abstract

Background:

Health care facilities are considering the use of reusable respiratory protective devices (RPDs) to mitigate a potential N95 filtering facepiece respirator shortage caused by an influenza pandemic. US regulators are also considering stockpiling reusable RPDs for pandemic preparedness, but limited data exist on the effectiveness of cleaning and disinfection of these devices. This study defines reprocessing protocols and evaluates their effectiveness against a pandemic influenza strain in a laboratory setting.

Methods:

Five half-mask elastomeric respirator models and 3 powered air-purifying respirator models were contaminated with influenza virus and artificial skin oil on multiple surfaces. RPDs were then manually treated with 1 of 2 methods: cleaned or cleaned and disinfected. Presence of viable influenza was determined via swab sampling and a median tissue culture infectious dose assay.

Results:

Across 41 RPD surfaces, a mean log reduction in viable influenza of 4.54 ±0.97 log10 median tissue culture infectious dose was achieved for all treated surfaces, which included both cleaned and cleaned and disinfected surfaces.

Conclusions:

The methods defined as part of this study are effective for eliminating viable influenza in the presence of artificial skin oil on most of the RPD surfaces tested. Material type and RPD design should be considered when implementing RPD reprocessing protocols.


Url:
DOI: 10.1016/j.ajic.2017.06.034
PubMed: 28844381
PubMed Central: 6193495

Links to Exploration step

PMC:6193495

Le document en format XML

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<title>Background:</title>
<p id="P1">Health care facilities are considering the use of reusable respiratory protective devices (RPDs) to mitigate a potential N95 filtering facepiece respirator shortage caused by an influenza pandemic. US regulators are also considering stockpiling reusable RPDs for pandemic preparedness, but limited data exist on the effectiveness of cleaning and disinfection of these devices. This study defines reprocessing protocols and evaluates their effectiveness against a pandemic influenza strain in a laboratory setting.</p>
</sec>
<sec id="S2">
<title>Methods:</title>
<p id="P2">Five half-mask elastomeric respirator models and 3 powered air-purifying respirator models were contaminated with influenza virus and artificial skin oil on multiple surfaces. RPDs were then manually treated with 1 of 2 methods: cleaned or cleaned and disinfected. Presence of viable influenza was determined via swab sampling and a median tissue culture infectious dose assay.</p>
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<title>Results:</title>
<p id="P3">Across 41 RPD surfaces, a mean log reduction in viable influenza of 4.54 ±0.97 log
<sub>10</sub>
median tissue culture infectious dose was achieved for all treated surfaces, which included both cleaned and cleaned and disinfected surfaces.</p>
</sec>
<sec id="S4">
<title>Conclusions:</title>
<p id="P4">The methods defined as part of this study are effective for eliminating viable influenza in the presence of artificial skin oil on most of the RPD surfaces tested. Material type and RPD design should be considered when implementing RPD reprocessing protocols.</p>
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Engineering Science Division, Applied Research Associates, Panama City, FL</aff>
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National Institute for Occupational Safety and Health, National Personal Protective Technology Laboratory, Pittsburgh, PA</aff>
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Address correspondence to Delbert A. Harnish, MS, Engineering Science Division, Applied Research Associates, 430 W 5th St, Ste 700, Panama City, FL 32401.
<email>dharnish@ara.com</email>
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<abstract id="ABS1">
<sec id="S1">
<title>Background:</title>
<p id="P1">Health care facilities are considering the use of reusable respiratory protective devices (RPDs) to mitigate a potential N95 filtering facepiece respirator shortage caused by an influenza pandemic. US regulators are also considering stockpiling reusable RPDs for pandemic preparedness, but limited data exist on the effectiveness of cleaning and disinfection of these devices. This study defines reprocessing protocols and evaluates their effectiveness against a pandemic influenza strain in a laboratory setting.</p>
</sec>
<sec id="S2">
<title>Methods:</title>
<p id="P2">Five half-mask elastomeric respirator models and 3 powered air-purifying respirator models were contaminated with influenza virus and artificial skin oil on multiple surfaces. RPDs were then manually treated with 1 of 2 methods: cleaned or cleaned and disinfected. Presence of viable influenza was determined via swab sampling and a median tissue culture infectious dose assay.</p>
</sec>
<sec id="S3">
<title>Results:</title>
<p id="P3">Across 41 RPD surfaces, a mean log reduction in viable influenza of 4.54 ±0.97 log
<sub>10</sub>
median tissue culture infectious dose was achieved for all treated surfaces, which included both cleaned and cleaned and disinfected surfaces.</p>
</sec>
<sec id="S4">
<title>Conclusions:</title>
<p id="P4">The methods defined as part of this study are effective for eliminating viable influenza in the presence of artificial skin oil on most of the RPD surfaces tested. Material type and RPD design should be considered when implementing RPD reprocessing protocols.</p>
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